drugset / Trial / NCT02859766

Safety and Pharmacokinetics of Abicipar Pegol Intravitreal Injections in Patients With Neovascular AMD

NCT02859766

Phase 1 Completed 30 enrolled Allergan
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate the safety and characterize the systemic pharmacokinetics (PK) of free and vascular endothelial growth factor (VEGF)-bound abicipar following single and multiple intravitreal injections of abicipar pegol in treatment-naïve patients with neovascular age-related macular degeneration (AMD).

Timeline

Start
2016-12-07
Primary completion
2017-10-20
Completion
2017-10-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Abicipar pegol Protein / enzyme biologic 2 mg Intravitreal

Indications